HEPARIN CAP, INJECTION CAP MALE LUER-
K-Number: K841772 · 1984-07-06
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Device Summary
Frequently Asked Questions
What is the HEPARIN CAP, INJECTION CAP MALE LUER-?
HEPARIN CAP, INJECTION CAP MALE LUER- is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Linton Biomed Corp.. The 510(k) number is K841772.
When did HEPARIN CAP, INJECTION CAP MALE LUER- receive FDA 510(k) clearance?
HEPARIN CAP, INJECTION CAP MALE LUER- received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841772.
Who is the listed applicant for HEPARIN CAP, INJECTION CAP MALE LUER-?
The FDA 510(k) record lists Linton Biomed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEPARIN CAP, INJECTION CAP MALE LUER-?
The FDA product code for HEPARIN CAP, INJECTION CAP MALE LUER- is FPA.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Linton Biomed Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FPA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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